HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390361Generated: October 27, 2026
Methanol → 1-N-methyl-4-nitrobenzene-1,2-diamine
https://huagongshe.com/reaction/1390361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | N-methyl-2,4-dinitroaniline | HCID 74891 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-N-methyl-4-nitrobenzene-1,2-diamine | HCID 3420025 | 94.4% |
Reaction Steps
71 Parts of 2,4-dinitro-N-methylaniline and 53 parts of sodium hydrogen carbonate are stirred in 144 parts of methanol. The yellow suspension is heated in the course of 20 minutes to 40° C. Simultaneously, 81.9 parts of 60% sodium sulphide are dissolved in 144 parts of water of approx. 40° C and 1.2 parts of 30% sodium hydroxide solution are added to the resultant solution. The turbid yellow solution is filtered. The clear yellow filtrate is added dropwise in the course of 2 hours to the suspension of 2,4-dinitro-N-methylaniline. An exothermic reaction occurs during the dropwise addition. The contents of the flask turn dark in colour. The new suspension is heated in the course of 1 hour to 70° C and stirred for 15 minutes at this temperature (reflux). Then 144 parts of methanol are distilled off. The residue is cooled to 25° C and 50 parts of ice are added. After suction filtration at 8° C, the filter cake is washed three times with 160 parts of water and dried in vacuo at 60° C, affording 56.8 parts of 2-amino-4-nitro-N-methylaniline (94.4% of theory). The melting point of the product is 177°-178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04138568 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-d7f27637653a41e0a1945b969a420bb7 |
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| Source note | uspto-grants-1979_02 |
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